Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,730 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,730 in last 12 months

Showing 1870118720 of 53,623 recalls

Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector L24mm Recalled by Aesculap Implant...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector L 42-58mm Recalled by Aesculap Implant...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector L22mm Recalled by Aesculap Implant...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector Recalled by Aesculap Implant Systems...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 5, 2020· COOLHAUS

Recalled Item: Coolhaus Awesome Ice Cream -That Dough Though Ice Cream Sandwich Recalled by...

The Issue: Package label does not declare soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 4, 2020· Toufayan Bakery, Inc.

Recalled Item: Goodie Girl Recalled by Toufayan Bakery, Inc. Due to Undeclared Wheat

The Issue: Gluten free product was mixed with wheat containing product. Undeclared Wheat.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 4, 2020· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine Transdermal System 5 mcg/hour Recalled by Teva Pharmaceuticals...

The Issue: Failed Stability Specifications: Below specification result for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc....

The Issue: Product not properly being aligned with the adequate gamma sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet Regenerex Primary Taper Cap Item Number 141269 Recalled by Biomet,...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055 Recalled by...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Braxton Medical Corporation

Recalled Item: B. Braun Introcan IV Safety Catheters Recalled by Braxton Medical...

The Issue: Recalled products do not have FDA approval for sale in the United States.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050 Recalled by Biomet,...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· AB ULAX

Recalled Item: 1500 Flex Heat and Moisture Exchanger Recalled by AB ULAX Due to Firm has...

The Issue: Firm has received 6 complaints that the Heat Moisture Exchanger (HME)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2020· Biomet, Inc.

Recalled Item: (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar...

The Issue: Zimmer Biomet is conducting a medical device recall for three lots of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 3, 2020· Akorn, Inc.

Recalled Item: Eye Itch Relief Recalled by Akorn, Inc. Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2020· pH-D Feminine Health

Recalled Item: pH-D Feminine Health Boric Acid Vaginal Suppositories Recalled by pH-D...

The Issue: Marketed without an Approved NDA/ANDA.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2020· Preferred Pharmaceuticals, Inc.

Recalled Item: Nature-Throid Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2020· Preferred Pharmaceuticals, Inc.

Recalled Item: Nature-Throid Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2020· Preferred Pharmaceuticals, Inc.

Recalled Item: Nature-Throid Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund